UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Mutually repressive interaction between Brn1/2 and Rorb contributes to the establishment of neocortical layer 2/3 and layer 4

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (12), p.3371-3376

2016

Volltextzugriff (PDF)

Transcriptional control of cone photoreceptor diversity by a thyroid hormone receptor

Proceedings of the National Academy of Sciences - PNAS, 2022-12, Vol.119 (49), p.e2209884119-e2209884119

2022

Volltextzugriff (PDF)

Identity of neocortical layer 4 neurons is specified through correct positioning into the cortex

eLife, 2016-02, Vol.5

2016

Volltextzugriff (PDF)

The COUP-TFII/Neuropilin-2 is a molecular switch steering diencephalon-derived GABAergic neurons in the developing mouse brain

Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (36), p.E4985-E4994

2015

Volltextzugriff (PDF)

Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome

Birth defects research. A Clinical and molecular teratology, 2007-01, Vol.79 (1), p.50-57

2007

Volltextzugriff (PDF)

Caudal Regression and Tracheoesophageal Malformation Induced by Adriamycin: A Novel Chick Model of VATER Association

Pediatric research, 2009-06, Vol.65 (6), p.607-612

2009

Volltextzugriff (PDF)

Retinoid-Related Orphan Receptor β and Transcriptional Control of Neuronal Differentiation

Current topics in developmental biology, 2017, Vol.125, p.227-255

2017

Volltextzugriff (PDF)

Identification of a prosencephalic-specific enhancer of SALL1: Comparative genomic approach using the chick embryo

Pediatric research, 2007-06, Vol.61 (6), p.660-665

2007

Volltextzugriff (PDF)

Neuronal Heterotopias Affect the Activities of Distant Brain Areas and Lead to Behavioral Deficits

The Journal of neuroscience, 2015-09, Vol.35 (36), p.12432-12445

2015

Volltextzugriff (PDF)

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations

The Journal of pediatrics, 2006-03, Vol.148 (3), p.410-414

2006

Volltextzugriff (PDF)

Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co‐activator CBFB

Congenital anomalies, 2004-12, Vol.44 (4), p.225-229

2004

Volltextzugriff (PDF)

S2C-24-1 Abnormal cortical architectures and neuropsychiatric disorders

Journal of Pharmacological Sciences, 2014-02, Vol.124 (suppl), p.47-47

2014

Volltextzugriff (PDF)

Upper airway obstruction in neonates and infants with CHARGE syndrome

American journal of medical genetics. Part A, 2007-08, Vol.143A (16), p.1815-1820

2007

Volltextzugriff (PDF)

Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype

American journal of medical genetics. Part A, 2008-08, Vol.146A (15), p.1967-1971

2008

Volltextzugriff (PDF)

An Alu retrotransposition‐mediated deletion of CHD7 in a patient with CHARGE syndrome

American journal of medical genetics. Part A, 2007-04, Vol.143A (7), p.721-726

2007

Volltextzugriff (PDF)

Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome

Birth defects research. A Clinical and molecular teratology, 2007-01, Vol.79 (1), p.50-57

2007

Volltextzugriff (PDF)

Iridic and retinal coloboma associated with prenatal methimazole exposure

American journal of medical genetics. Part A, 2005-12, Vol.139A (2), p.156-158

2005

Volltextzugriff (PDF)

Screening for CHARGE syndrome mutations in the CHD7 gene using denaturing high-performance liquid chromatography

Genetic testing, 2006, Vol.10 (4), p.244-251

2006

Volltextzugriff (PDF)

Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatography

Genetic testing, 2005-06, Vol.9 (2), p.85-92

2005

Volltextzugriff (PDF)

Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype

American Journal of Medical Genetics Part A, 2008, Vol.146A (15), p.1967-1971

2008

Volltextzugriff (PDF)

Iridic and retinal coloboma associated with prenatal methimazole exposure

American journal of medical genetics, 2005, Vol.139A (2), p.156-158

2005

Volltextzugriff (PDF)

An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndrome

American Journal of Medical Genetics Part A, 2007, Vol.143A (7), p.721-726

2007

Volltextzugriff (PDF)

Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB

Congenital Anomalies, 2004, Vol.44 (4), p.225-229

2004

Volltextzugriff (PDF)

Effect of chrysanthemum flower extract on proliferation of various cancer cell lines

Nippon Shokuhin Kagaku Kogaku Kaishi, 2003/10/15, Vol.50(10), pp.493-497

2003

Volltextzugriff (PDF)

1 – 25 von 25

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(22)
Berichte
(3)

Sprache

Englisch
(23)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

Science & Technology
(18)
Life Sciences & Biomedicine
(15)
Humans
(12)
Animals
(10)
Biological And Medical Sciences
(7)
Medical Sciences
(7)
Dna-Binding Proteins - Genetics
(6)
Genetics & Heredity
(6)
Dna Helicases - Genetics
(5)
Female
(5)
Medical Genetics
(5)
Mice
(5)
Abnormalities, Multiple - Genetics
(4)
Charge Syndrome
(4)
Heart Defects, Congenital - Genetics
(4)
Infant, Newborn
(4)
Syndrome
(4)
Binding Sites
(3)
Biological Sciences
(3)
Cell Fate
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutually repressive interaction between Brn1/2 and Rorb contributes to the establishment of neocortical layer 2/3 and layer 4

Transcriptional control of cone photoreceptor diversity by a thyroid hormone receptor

Identity of neocortical layer 4 neurons is specified through correct positioning into the cortex

The COUP-TFII/Neuropilin-2 is a molecular switch steering diencephalon-derived GABAergic neurons in the developing mouse brain

Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome

Caudal Regression and Tracheoesophageal Malformation Induced by Adriamycin: A Novel Chick Model of VATER Association

Retinoid-Related Orphan Receptor β and Transcriptional Control of Neuronal Differentiation

Identification of a prosencephalic-specific enhancer of SALL1: Comparative genomic approach using the chick embryo

Neuronal Heterotopias Affect the Activities of Distant Brain Areas and Lead to Behavioral Deficits

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations

Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co‐activator CBFB

Association of impaired neuronal migration with cognitive deficits in extremely preterm infants

S2C-24-1 Abnormal cortical architectures and neuropsychiatric disorders

Upper airway obstruction in neonates and infants with CHARGE syndrome

Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype

An Alu retrotransposition‐mediated deletion of CHD7 in a patient with CHARGE syndrome

Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome

Iridic and retinal coloboma associated with prenatal methimazole exposure

Screening for CHARGE syndrome mutations in the CHD7 gene using denaturing high-performance liquid chromatography

Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatography

Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype

Iridic and retinal coloboma associated with prenatal methimazole exposure

An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndrome

Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB

Effect of chrysanthemum flower extract on proliferation of various cancer cell lines

Suchergebnisse filtern